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Molecular Psychiatry|February 13, 2024
Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samplesAsbjørn Holmgren, Ibrahim Akkouh, Kevin Sean O'Connell, et al.
Translational Psychiatry|January 29, 2022
Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brainAsbjørn Holmgren, Lars Hansson, Kristine Bjerkaas-Kjeldal, et al.
European Journal of Medical Genetics|June 10, 2014
Haploinsufficiency of XPO1 and USP34 by a de novo 230 kb deletion in 2p15, in a patient with mild intellectual disability and cranio-facial dysmorphismsMadeleine Fannemel, Tuva Barøy, Asbjørn Holmgren, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3BChristeen Ramane J Pedurupillay, Tuva Barøy, Asbjørn Holmgren, et al.
Genes|December 6, 2016
Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 PhenotypeNadia Skauli, Sean Wallace, Samuel C C Chiang, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|October 26, 2019
Exploring lithium's transcriptional mechanisms of action in bipolar disorder: a multi-step studyIbrahim A Akkouh, Silje Skrede, Asbjørn Holmgren, et al.
The Plant Cell|July 29, 2008
The EPIP peptide of INFLORESCENCE DEFICIENT IN ABSCISSION is sufficient to induce abscission in arabidopsis through the receptor-like kinases HAESA and HAESA-LIKE2Grethe-Elisabeth Stenvik, Nora M Tandstad, Yongfeng Guo, et al.
Plos One|January 28, 2014
Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletionsIselin Marie Wedding, Jeanette Koht, Gia Tuong Tran, et al.
Orphanet Journal of Rare Diseases|January 9, 2013
Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disabilityTuva Barøy, Doriana Misceo, Petter Strømme, et al.
Neuromuscular Disorders : NMD|July 25, 2016
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2Christeen Ramane J Pedurupillay, Silja S Amundsen, Tuva Barøy, et al.
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